Overrepresentation of pregnancies conceived by artificial reproductive technology in prenatally identified fetuses with Beckwith-Wiedemann syndrome
暂无分享,去创建一个
Amy Crunk | John P. Johnson | Abdallah F Elias | J. Schoof | L. Beischel | C. Schwanke | Abdallah F. Elias | Katie Styren | Corbin M Schwanke
[1] J. Martin,et al. Births: Final Data for 2016. , 2018, National vital statistics reports : from the Centers for Disease Control and Prevention, National Center for Health Statistics, National Vital Statistics System.
[2] M. Carella,et al. Assisted Reproductive Techniques and Risk of Beckwith-Wiedemann Syndrome , 2017, Pediatrics.
[3] E. Wong,et al. Altered gene expression of H19 and IGF2 in placentas from ART pregnancies. , 2015, Placenta.
[4] H. Hiura,et al. Imprinting methylation errors in ART , 2014, Reproductive medicine and biology.
[5] John P. Johnson,et al. Genome‐wide androgenetic mosaicism , 2014, Clinical genetics.
[6] S. Elalaoui,et al. Maternal Hypomethylation of KvDMR in a Monozygotic Male Twin Pair Discordant for Beckwith-Wiedemann Syndrome , 2013, Molecular Syndromology.
[7] J. Qiao,et al. Embryo Manipulation and Imprinting , 2012, Seminars in Reproductive Medicine.
[8] B. Källén,et al. Trends in delivery and neonatal outcome after in vitro fertilization in Sweden: data for 25 years. , 2010, Human reproduction.
[9] A. Westerveld,et al. Lessons from BWS twins: complex maternal and paternal hypomethylation and a common source of haematopoietic stem cells , 2009, European Journal of Human Genetics.
[10] J. Segars,et al. Imprinting disorders and assisted reproductive technology. , 2009, Fertility and sterility.
[11] L. Wilkins-Haug,et al. Isolated fetal omphalocele, Beckwith-Wiedemann syndrome, and assisted reproductive technologies. , 2009, Birth defects research. Part A, Clinical and molecular teratology.
[12] T. Eggermann,et al. IGF2/H19 hypomethylation in Silver–Russell syndrome and isolated hemihypoplasia , 2008, European Journal of Human Genetics.
[13] W. Reardon,et al. A survey of assisted reproductive technology births and imprinting disorders , 2007 .
[14] R. Hennekam,et al. Infertility, assisted reproduction technologies and imprinting disturbances: a Dutch study. , 2007, Human reproduction.
[15] L. Laurino,et al. Chromosome 11 segmental paternal isodisomy in amniocytes from two fetuses with omphalocoele: new highlights on phenotype–genotype correlations in Beckwith–Wiedemann syndrome , 2007, Journal of Medical Genetics.
[16] A. Holland,et al. Changing rates of genetic subtypes of Prader–Willi syndrome in the UK , 2007, European Journal of Human Genetics.
[17] S. Warren,et al. Molecular diagnosis of Beckwith-Wiedemann Syndrome using quantitative methylation-sensitive polymerase chain reaction , 2006, Genetics in Medicine.
[18] R. Siebert,et al. A maternal hypomethylation syndrome presenting as transient neonatal diabetes mellitus , 2006, Human Genetics.
[19] W. Reardon,et al. Assisted reproductive therapies and imprinting disorders--a preliminary British survey. , 2006, Human reproduction.
[20] M. Butler,et al. Prader–Willi syndrome: clinical genetics, cytogenetics and molecular biology , 2005, Expert Reviews in Molecular Medicine.
[21] A. Pinborg,et al. Imprinting diseases and IVF: Danish National IVF cohort study. , 2005, Human reproduction.
[22] Michael F. Wangler,et al. Association between Beckwith-Wiedemann syndrome and assisted reproductive technology: a case series of 19 patients. , 2005, Fertility and sterility.
[23] J. Halliday,et al. Beckwith-Wiedemann syndrome and IVF: a case-control study. , 2004, American journal of human genetics.
[24] T. Bestor. Imprinting errors and developmental asymmetry. , 2003, Philosophical transactions of the Royal Society of London. Series B, Biological sciences.
[25] Antoine Flahault,et al. In vitro fertilization may increase the risk of Beckwith-Wiedemann syndrome related to the abnormal imprinting of the KCN1OT gene. , 2003, American journal of human genetics.
[26] W. Reik,et al. Beckwith-Wiedemann syndrome and assisted reproduction technology (ART) , 2003, Journal of medical genetics.
[27] K. Buiting,et al. Another case of imprinting defect in a girl with Angelman syndrome who was conceived by intracytoplasmic semen injection. , 2003, American journal of human genetics.
[28] Andrew P Feinberg,et al. Association of in vitro fertilization with Beckwith-Wiedemann syndrome and epigenetic alterations of LIT1 and H19. , 2003, American journal of human genetics.
[29] Bai-Lin Wu,et al. Intracytoplasmic sperm injection may increase the risk of imprinting defects. , 2002, American journal of human genetics.
[30] R. Weksberg,et al. Discordant KCNQ1OT1 imprinting in sets of monozygotic twins discordant for Beckwith-Wiedemann syndrome. , 2002, Human molecular genetics.
[31] J. Ruijter,et al. Increased tumour risk for BWS patients correlates with aberrant H19 and not KCNQ1OT1 methylation: occurrence of KCNQ1OT1 hypomethylation in familial cases of BWS. , 2001, Human molecular genetics.
[32] D. J. Driscoll,et al. A maternally methylated CpG island in KvLQT1 is associated with an antisense paternal transcript and loss of imprinting in Beckwith-Wiedemann syndrome. , 1999, Proceedings of the National Academy of Sciences of the United States of America.
[33] A. Feinberg,et al. LIT1, an imprinted antisense RNA in the human KvLQT1 locus identified by screening for differentially expressed transcripts using monochromosomal hybrids. , 1999, Human molecular genetics.
[34] A. Feinberg,et al. Loss of imprinting of a paternally expressed transcript, with antisense orientation to KVLQT1, occurs frequently in Beckwith-Wiedemann syndrome and is independent of insulin-like growth factor II imprinting. , 1999, Proceedings of the National Academy of Sciences of the United States of America.
[35] I. Temple,et al. Clinical features and natural history of Beckwith‐Wiedemann syndrome: presentation of 74 new cases , 1994, Clinical genetics.
[36] D. J. Driscoll,et al. Functional imprinting and epigenetic modification of the human SNRPN gene. , 1993, Human molecular genetics.
[37] A. Razin,et al. Developmental pattern of gene-specific DNA methylation in the mouse embryo and germ line. , 1992, Genes & development.